Archives for Chemistry Experiments of 1416134-49-0

This literature about this compound(1416134-49-0)Electric Literature of C13H19N3O2has given us a lot of inspiration, and I hope that the research on this compound((2S,5R)-5-((Benzyloxy)amino)piperidine-2-carboxamide) can be further advanced. Maybe we can get more compounds in a similar way.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 1416134-49-0, is researched, Molecular C13H19N3O2, about Use of Lipase Catalytic Resolution in the Preparation of Ethyl (2S,5R)-5-((Benzyloxy)amino)piperidine-2-carboxylate, a Key Intermediate of the β-Lactamase Inhibitor Avibactam, the main research direction is lipase ethyl benzyloxyaminopiperidinecarboxylate intermediate lactamase inhibitor avibactam.Electric Literature of C13H19N3O2.

Here we describe an efficient and cost-effective chemoenzymic synthesis of the β-lactamase inhibitor avibactam starting from com. available Et 5-hydroxypicolinate hydrochloride. Avibactam was synthesized in 10 steps with an overall yield of 23.9%. The synthetic route features a novel lipase-catalyzed resolution step during the preparation of (2S,5S)-Et 5-hydroxypiperidine-2-carboxylate, a valuable precursor of the key intermediate Et (2S,5R)-5-((benzyloxy)amino)piperidine-2-carboxylate. Our synthetic route was used to produce 400 g of avibactam sodium salt.

This literature about this compound(1416134-49-0)Electric Literature of C13H19N3O2has given us a lot of inspiration, and I hope that the research on this compound((2S,5R)-5-((Benzyloxy)amino)piperidine-2-carboxamide) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica